SYNTHETIC POWEDERED VINYL EXAMINATION GLOVES
K-Number: K050455 · 2005-03-29
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Device Summary
Frequently Asked Questions
What is the SYNTHETIC POWEDERED VINYL EXAMINATION GLOVES?
SYNTHETIC POWEDERED VINYL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2005-03-29. The listed applicant is Zibo Blue Intco Plastic & Rubber Products Co., Ltd.. The 510(k) number is K050455.
When did SYNTHETIC POWEDERED VINYL EXAMINATION GLOVES receive FDA 510(k) clearance?
SYNTHETIC POWEDERED VINYL EXAMINATION GLOVES received FDA 510(k) clearance on 2005-03-29, under 510(k) number K050455.
Who is the listed applicant for SYNTHETIC POWEDERED VINYL EXAMINATION GLOVES?
The FDA 510(k) record lists Zibo Blue Intco Plastic & Rubber Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHETIC POWEDERED VINYL EXAMINATION GLOVES?
The FDA product code for SYNTHETIC POWEDERED VINYL EXAMINATION GLOVES is LYZ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Zibo Blue Intco Plastic & Rubber Products Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LYZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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